2-[2-(2-Azidoethoxy)ethoxy]ethanol - ≥95% , CAS No.86520-52-7

CAS: 86520-52-7 Cat. No.: A136914 Formule: C6H13N3O3 Poids moléculaire: 175.19 Beilstein Registry Number: 4418543 Numéro CE: 694-430-1
DISPONIBLE À COMMANDE
GRADE & PURITY ≥95%
Synonyms
1-Azido-8-hydroxy-3,6-dioxaoctane | SCHEMBL214423 | Ethanol, 2-[2-(2-azidoethoxy)ethoxy]- | 2-(2-(2-azidoethoxy)ethoxy)ethan-1-ol | BP-20693 | 8-Azido-3,6-dioxaoctanol | 2-(2-(2-AZIDOETHOXY)ETHOXY)ETHANOL | LCZC464 | ZB0973 | 5-Pentylpent-2-en-5-olide | G
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
Application
Antibody Drug Conjugates(ADC), Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo
★
Size
Allemagne (EU)
USA*
Price
Qty
250mg
A136914-250mg
—
3 En stock
58,05€
1g
A136914-1g
—
3 En stock
109,25€
5g
A136914-5g
—
2 En stock
461,55€
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
1-Azido-8-hydroxy-3,6-dioxaoctane | SCHEMBL214423 | Ethanol, 2-[2-(2-azidoethoxy)ethoxy]- | 2-(2-(2-azidoethoxy)ethoxy)ethan-1-ol | BP-20693 | 8-Azido-3,6-dioxaoctanol | 2-(2-(2-AZIDOETHOXY)ETHOXY)ETHANOL | LCZC464 | ZB0973 | 5-Pentylpent-2-en-5-olide | G
Spécifications et pureté
≥95%
Conditions de stockage de stockage
Store at 2-8°C,Protected from light,Argon charged
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Pureté
≥95%
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488197047
Sourires canoniques
C(COCCOCCO)N=[N+]=[N-]
IUPAC Name
2-[2-(2-azidoethoxy)ethoxy]ethanol
InChIKey
PMNIHDBMMDOUPD-UHFFFAOYSA-N
INCHI
1S/C6H13N3O3/c7-9-8-1-3-11-5-6-12-4-2-10/h10H,1-6H2
Isomères SMILES
C(COCCOCCO)N=[N+]=[N-]
WGK Allemagne
3
Poids moléculaire
175.19
Beilstein
4418543
Reaxy-Rn
4418543
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4418543&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic 1,3-dipolar compounds
ClasseAllyl-type 1,3-dipolar organic compounds
SubclassAzo imides
Intermediate Tree Nodes Not available
Direct ParentAzo imides
Alternative Parents Azo compounds  Dialkyl ethers  Primary alcohols  Organopnictogen compounds  Organic zwitterions  Organic salts  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Azo imide - Azo compound - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organic zwitterion - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as azo imides. These are n-Imides of azo compounds, analogous to azoxy compounds, having a delocalized structure.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDateArticle
C2306605Certificate of AnalysisSep 01, 2026 A136914
C2306604Certificate of AnalysisSep 01, 2026 A136914
K2201031Certificate of AnalysisMay 11, 2026 A136914
K2201032Certificate of AnalysisMay 11, 2026 A136914
K2201034Certificate of AnalysisMay 11, 2026 A136914
J2126013Certificate of AnalysisMay 09, 2025 A136914
J2126014Certificate of AnalysisMay 09, 2025 A136914
Propriétés chimiques et physiques
SensibilitéLight sensitive
Poids moléculaire175.190 g/mol
XLogP30.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count8
Exact Mass175.096 Da
Monoisotopic Mass175.096 Da
Topological Polar Surface Area53.100 Ų
Heavy Atom Count12
Formal Charge0
Complexity136.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Click Chemistry in Drug Discovery
Copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC)
Reactions of strained alkenes in click chemistry
Strain-promoted alkyne-nitrone cycloaddition (SPANC)
Strain-promoted alkyne-nitrone cycloaddition (SPANC)
Potential Applications in Click Chemistry
Click Chemistry
The application of click chemistry in chemical ligation and peptide modification
Calculateurs de solution
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